Roche

Manufacturing Equipment Engineer

Roche$81K — $151K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Bioengineering, Automation Engineering, Biology, Biochemistry, or related field.
  • 5+ years of experience in utility system and equipment engineering in biotech or clinical lab settings.
  • Hands-on experience with environmental monitoring systems (e.g., REES, ViewLinc).
  • Direct experience in cGMP/cGXP or ISO-regulated environments, ideally with FDA/BSI audits.
  • Familiarity with lab automation and clinical devices, including liquid handlers and imaging systems.

Responsibilities

  • Administer and control the Environmental Monitoring System (EMS) for data integrity and operational reliability.
  • Lead resolution of equipment Non-Conformances (NCs) and conduct Root Cause Analysis (RCA).
  • Support internal quality reviews and external regulatory audits with technical documentation and equipment records.
  • Plan and execute preventive maintenance and corrective measures for site equipment and utility systems.
  • Oversee installation, troubleshooting, and Commissioning & Qualification (C&Q) programs for critical lab infrastructure.
  • Manage vendor relationships to optimize service and prolong equipment lifespan.
  • Provide training and administration of system access for site Standard Operating Procedures (SOPs).

Benefits

  • Health, dental, and vision insurance options.
  • Discretionary annual bonuses based on individual and company performance.
  • Retirement plan options to support long-term planning.
  • Opportunities for professional development and continuing education.
Full Job Description
The Position

Are you an agile engineering professional looking to keep cutting-edge life sciences laboratories operating at peak performance? Join our cross-functional site network across Santa Clara and Pleasanton as a Manufacturing Equipment Engineer. In this high-impact role, you will safeguard our facility's "Right to Operate" by managing critical laboratory infrastructure, ensuring continuous regulatory compliance, and maximizing system uptime. By serving as the core technical leader for our Environmental Monitoring System (EMS) and quality risk management, your expertise will directly ensure data integrity, operational efficiency, and product quality in a regulated environment.

The Opportunity

As a Manufacturing Equipment Engineer, you will serve as the system controller and administrator for the site’s Environmental Monitoring System (EMS), overseeing everything from database administration and alert matrices to software maintenance and sensor allocation. Beyond EMS stewardship, you will drive total equipment lifecycle management across clinical and facility infrastructure—including liquid handling devices, CTUs, and imaging systems—by leading calibrations, preventive maintenance, and troubleshooting. Working closely with quality teams, you will champion Non-Conformance (NC) investigations, execute Root Cause Analysis (RCA) in SAP, and provide front-facing technical support during high-stakes FDA and BSI regulatory audits.

  • EMS Administration & Control: Serve as the primary system controller for the Environmental Monitoring System (EMS), overseeing database settings, sensor allocations, CTU mapping, alert matrices, and annual software upkeep to ensure 24/7 data integrity.

  • Non-Conformance & RCA Leadership: Drive end-to-end lifecycle resolution of equipment Non-Conformances (NCs), deviations, and Out-of-Specification (OOS) calibration events, executing robust Root Cause Analysis (RCA) and impact assessments in corporate QMS portals (SAP).

  • Audit & Compliance Support: Provide direct technical front-room and backroom support during internal quality reviews and external regulatory audits (e.g., FDA, BSI) by assembling critical equipment records and excursion logs.

  • Equipment Lifecycle & Maintenance: Plan, validate, calibrate, and perform preventive and corrective maintenance across site equipment and utility systems to minimize operational downtime.

  • Infrastructure & Commissioning Support: Oversee the installation, troubleshooting, and C&Q (Commissioning & Qualification) programs for CTUs, process utilities, and facility systems, continuously analyzing system status trends for improvements.

  • Vendor & Budget Oversight: Direct external vendor management to control costs, guarantee service deliverability, minimize safety risks, and extend asset life across contractual lifecycles.

  • Site Training & Administration: Manage system access credentials, conduct technical software training, and act as a qualified trainer for site C&Q Standard Operating Procedures (SOPs).

Who You Are

  • Educational Background: Bachelor’s degree in Bioengineering, Automation Engineering, Biology, Biochemistry, or equivalent practical experience.

  • Biotech Industry Experience: 5+ years of robust background in utility system and equipment engineering within a biotechnology or clinical laboratory environment.

  • Hands-on EMS Administration: Proven track record administering and controlling continuous environmental monitoring system networks (e.g., REES, ViewLinc) including alarm processing and parameter change management.

  • Regulatory Compliance & Audits: Direct experience working within cGMP/cGXP or ISO-regulated environments, with a preference for demonstrated support during FDA or BSI inspections.

  • Lab Automation & Device Expertise: Practical experience maintaining, deploying, or troubleshooting clinical lab devices, automated liquid handlers, imaging systems, and facility CTUs.

This position is not eligible for relocation.

The expected salary range for this position based on the primary location of California is $81,500 - $151,300 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.

 

 

About Roche

Roche Holding AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel. Roche is the largest pharmaceutical company in the world, and the leading provider of cancer treatments globally. The company also produces a range of diagnostic tests for medical professionals and patients. Roche was one of the first companies to bring targeted treatments to patients. In 2019, Roche had over 100,000 employees worldwide, and generated revenue of CHF 61.5 billion.
Learn more about Roche
Size
100,920 employees
Industry
NASDAQ

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